US11903998B2ActiveUtilityA1
Compositions and methods of treating cancer using lipid agonists and receptors thereof
Assignee: FORSYTH DENTAL INFIRMARY FOR CHILDRENPriority: May 27, 2016Filed: May 25, 2017Granted: Feb 20, 2024
Est. expiryMay 27, 2036(~9.9 yrs left)· nominal 20-yr term from priority
A61K 38/177A61K 9/0019A61K 31/202A61K 33/243A61K 45/06A61P 35/00A61K 38/1793A61K 31/555
53
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Claims
Abstract
Provided herein are methods for preventing or treating cancer in a subject comprising overexpressing at least one Receptor for a lipid agonist, such as G-protein receptors for Resolvin. Such methods may be combined with administering Resolvins, or lipoxins and their analogs, of said Receptors to enhance the pro-resolution effects of the Resolvins, or lipoxins and their analogs, in the local, inflammatory environment where cancer cells are already present.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1. A method for treating lung cancer in a subject, wherein the subject comprises cells that overexpress Receptor for Resolvin E1 (ERV1), the method comprising:
administering at least one Resolvin E series lipid agonist to the subject, wherein the at least one Resolvin E series lipid agonist is selected from the group consisting of di-hydroxy members of the Resolvin E series and tri-hydroxy members of the Resolvin E series.
2. The method of claim 1 , wherein the at least one Resolvin E series lipid agonist is selected from the group consisting of Resolvin E1, Resolvin E2, and Resolvin E3.
3. The method of claim 1 , wherein the at least one Resolvin E series lipid agonist comprises Resolvin E 1.
4. The method of claim 1 , wherein the at least one Resolvin E series lipid agonist is administered systemically, wherein the systemic administration is selected from the group consisting of oral, intravenous, intradermal, intraperitoneal, subcutaneous, and intramuscular administration.
5. The method of claim 1 , wherein the at least one Resolvin E series lipid agonist is administered intratumorally or peritumorally.
6. The method of claim 1 , wherein the subject is treated with at least one additional anti-cancer agent, wherein the anti-cancer agent is selected from the group consisting of paclitaxel, cisplatin, topotecan, gemcitabine, bleomycin, etoposide, carboplatin, docetaxel, doxorubicin, topotecan, cyclophosphamide, trabectedin, olaparib, tamoxifen, letrozole, and bevacizumab.
7. The method of claim 1 , wherein the subject is concurrently treated with cisplatin.
8. The method of claim 1 , wherein the subject is treated with at least one additional anti-cancer therapy, wherein the anti-cancer therapy is radiation therapy, chemotherapy, or surgery.
9. The method of claim 1 , wherein the subject is a mammal.
10. The method of claim 1 , wherein the subject is a human.
11. The method of claim 1 , wherein an inflammatory response is inhibited or reduced in the subject, wherein the inhibition or reduction in the inflammatory response results in a decreased expression of the NF-κB, IL-6, and IL-8 genes.
12. The method of claim 1 , wherein an angiogenic response is inhibited or reduced in the subject, wherein the inhibition or reduction in the angiogenic response results in a decreased expression of the Ang1, Ang2, and VEGF genes.
13. The method of claim 1 , wherein malignancy is inhibited or reduced in the subject.
14. The method of claim 1 , wherein tumor necrosis is enhanced or increased in the subject.Cited by (0)
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